<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Martin K</submitter><funding>NIA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>U.S. Department of Defense</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><funding>Division of Graduate Education</funding><pagination>4452-4461</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8945255</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(9)</volume><pubmed_abstract>Recent advances in sample preparation enable label-free mass spectrometry (MS)-based proteome profiling of small numbers of mammalian cells. However, specific devices are often required to downscale sample processing volume from the standard 50-200 μL to sub-μL for effective nanoproteomics, which greatly impedes the implementation of current nanoproteomics methods by the proteomics research community. Herein, we report a facile one-pot nanoproteomics method termed SOPs-MS (&lt;u>s&lt;/u>urfactant-assisted &lt;u>o&lt;/u&gt;ne-&lt;u>p&lt;/u>ot sample processing at the &lt;u>s&lt;/u>tandard volume coupled with MS) for convenient robust proteome profiling of 50-1000 mammalian cells. Building upon our recent development of SOPs-MS for label-free single-cell proteomics at a low μL volume, we have systematically evaluated </pubmed_abstract><journal>Journal of proteome research</journal><pubmed_title>Facile One-Pot Nanoproteomics for Label-Free Proteome Profiling of 50-1000 Mammalian Cells.</pubmed_title><pmcid>PMC8945255</pmcid><funding_grant_id>U54CA217378</funding_grant_id><funding_grant_id>P41GM103493</funding_grant_id><funding_grant_id>W81XWH-16-1-0021</funding_grant_id><funding_grant_id>U01 DK121289</funding_grant_id><funding_grant_id>U19 AG065156</funding_grant_id><funding_grant_id>R21 CA223715</funding_grant_id><funding_grant_id>T32 CA009054</funding_grant_id><funding_grant_id>UG3CA256967</funding_grant_id><funding_grant_id>U01CA227544</funding_grant_id><funding_grant_id>U01 CA227544</funding_grant_id><funding_grant_id>P41 GM103493</funding_grant_id><funding_grant_id>U54 CA217378</funding_grant_id><funding_grant_id>R21CA223715</funding_grant_id><funding_grant_id>R01GM090056</funding_grant_id><funding_grant_id>UG3 CA256967</funding_grant_id><funding_grant_id>P30 CA062203</funding_grant_id><funding_grant_id>DGE-1321846</funding_grant_id><funding_grant_id>P41 GM103533</funding_grant_id><funding_grant_id>P30CA062203</funding_grant_id><pubmed_authors>Qian WJ</pubmed_authors><pubmed_authors>Lin TT</pubmed_authors><pubmed_authors>Smith RD</pubmed_authors><pubmed_authors>Chrisler WB</pubmed_authors><pubmed_authors>Waterman ML</pubmed_authors><pubmed_authors>Sontag RL</pubmed_authors><pubmed_authors>Yang B</pubmed_authors><pubmed_authors>Shi T</pubmed_authors><pubmed_authors>Lu YJ</pubmed_authors><pubmed_authors>Rodland KD</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Orton DJ</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Tsai CF</pubmed_authors><pubmed_authors>Martin K</pubmed_authors><pubmed_authors>Zhao R</pubmed_authors><pubmed_authors>Wiley HS</pubmed_authors><pubmed_authors>Habowski AN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Facile One-Pot Nanoproteomics for Label-Free Proteome Profiling of 50-1000 Mammalian Cells.</name><description>Recent advances in sample preparation enable label-free mass spectrometry (MS)-based proteome profiling of small numbers of mammalian cells. However, specific devices are often required to downscale sample processing volume from the standard 50-200 μL to sub-μL for effective nanoproteomics, which greatly impedes the implementation of current nanoproteomics methods by the proteomics research community. Herein, we report a facile one-pot nanoproteomics method termed SOPs-MS (&lt;u>s&lt;/u>urfactant-assisted &lt;u>o&lt;/u&gt;ne-&lt;u>p&lt;/u>ot sample processing at the &lt;u>s&lt;/u>tandard volume coupled with MS) for convenient robust proteome profiling of 50-1000 mammalian cells. Building upon our recent development of SOPs-MS for label-free single-cell proteomics at a low μL volume, we have systematically evaluated </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-04T07:45:29.895Z</modification><creation>2025-04-04T07:45:29.895Z</creation></dates><accession>S-EPMC8945255</accession><cross_references><pubmed>34351778</pubmed><doi>10.1021/acs.jproteome.1c00403</doi></cross_references></HashMap>